EP0525994B1 - Tintenzusammensetzungen für das Ink-Jet-Schreibverfahren - Google Patents
Tintenzusammensetzungen für das Ink-Jet-Schreibverfahren Download PDFInfo
- Publication number
- EP0525994B1 EP0525994B1 EP92306061A EP92306061A EP0525994B1 EP 0525994 B1 EP0525994 B1 EP 0525994B1 EP 92306061 A EP92306061 A EP 92306061A EP 92306061 A EP92306061 A EP 92306061A EP 0525994 B1 EP0525994 B1 EP 0525994B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- ink
- percent
- weight
- ink composition
- yellow
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
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- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- VPTLINAJFCLEEI-UHFFFAOYSA-N [Na].[Na].[Na].NCCCCCN Chemical compound [Na].[Na].[Na].NCCCCCN VPTLINAJFCLEEI-UHFFFAOYSA-N 0.000 description 1
- CITHMWNQCVRPGG-UHFFFAOYSA-N [Na].[Na].[Na].NCCN Chemical compound [Na].[Na].[Na].NCCN CITHMWNQCVRPGG-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
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- 239000002250 absorbent Substances 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- DYRDKSSFIWVSNM-UHFFFAOYSA-N acetoacetanilide Chemical class CC(=O)CC(=O)NC1=CC=CC=C1 DYRDKSSFIWVSNM-UHFFFAOYSA-N 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
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- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000001000 anthraquinone dye Chemical class 0.000 description 1
- 229940045713 antineoplastic alkylating drug ethylene imines Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QFFVPLLCYGOFPU-UHFFFAOYSA-N barium chromate Chemical compound [Ba+2].[O-][Cr]([O-])(=O)=O QFFVPLLCYGOFPU-UHFFFAOYSA-N 0.000 description 1
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical class C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 150000004074 biphenyls Chemical class 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229960001506 brilliant green Drugs 0.000 description 1
- HXCILVUBKWANLN-UHFFFAOYSA-N brilliant green cation Chemical compound C1=CC(N(CC)CC)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](CC)CC)C=C1 HXCILVUBKWANLN-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
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- HFIYIRIMGZMCPC-UHFFFAOYSA-J chembl1326377 Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(N=NC=3C=CC(=CC=3)S(=O)(=O)CCOS([O-])(=O)=O)C(O)=C2C(N)=C1N=NC1=CC=C(S(=O)(=O)CCOS([O-])(=O)=O)C=C1 HFIYIRIMGZMCPC-UHFFFAOYSA-J 0.000 description 1
- JBTHDAVBDKKSRW-UHFFFAOYSA-N chembl1552233 Chemical compound CC1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 JBTHDAVBDKKSRW-UHFFFAOYSA-N 0.000 description 1
- ZLFVRXUOSPRRKQ-UHFFFAOYSA-N chembl2138372 Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ZLFVRXUOSPRRKQ-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- VDQQXEISLMTGAB-UHFFFAOYSA-N chloramine T Chemical compound [Na+].CC1=CC=C(S(=O)(=O)[N-]Cl)C=C1 VDQQXEISLMTGAB-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- VVOLVFOSOPJKED-UHFFFAOYSA-N copper phthalocyanine Chemical compound [Cu].N=1C2=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC=1C1=CC=CC=C12 VVOLVFOSOPJKED-UHFFFAOYSA-N 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
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- HNPZBDFFHBHBFR-UHFFFAOYSA-L disodium 5-[[4-(2-bromoprop-2-enoylamino)-2-sulfonatophenyl]diazenyl]-4-hydroxy-6-(methylamino)naphthalene-2-sulfonate Chemical compound [Na+].[Na+].CNc1ccc2cc(cc(O)c2c1N=Nc1ccc(NC(=O)C(Br)=C)cc1S([O-])(=O)=O)S([O-])(=O)=O HNPZBDFFHBHBFR-UHFFFAOYSA-L 0.000 description 1
- HJORILXJGREZJU-UHFFFAOYSA-L disodium 7-[(5-chloro-2,6-difluoropyrimidin-4-yl)amino]-4-hydroxy-3-[(4-methoxy-2-sulfonatophenyl)diazenyl]naphthalene-2-sulfonate Chemical compound ClC=1C(=NC(=NC1F)F)NC1=CC=C2C(=C(C(=CC2=C1)S(=O)(=O)[O-])N=NC1=C(C=C(C=C1)OC)S(=O)(=O)[O-])O.[Na+].[Na+] HJORILXJGREZJU-UHFFFAOYSA-L 0.000 description 1
- BMAUDWDYKLUBPY-UHFFFAOYSA-L disodium;3-[[4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2-methylphenyl]diazenyl]naphthalene-1,5-disulfonate Chemical compound [Na+].[Na+].C=1C=C(N=NC=2C=C3C(=CC=CC3=C(C=2)S([O-])(=O)=O)S([O-])(=O)=O)C(C)=CC=1NC1=NC(Cl)=NC(Cl)=N1 BMAUDWDYKLUBPY-UHFFFAOYSA-L 0.000 description 1
- YJHDFAAFYNRKQE-YHPRVSEPSA-L disodium;5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfonatophenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S([O-])(=O)=O)=CC=2)S([O-])(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 YJHDFAAFYNRKQE-YHPRVSEPSA-L 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005686 electrostatic field Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- WTIFIAZWCCBCGE-UUOKFMHZSA-N guanosine 2'-monophosphate Chemical compound C1=2NC(N)=NC(=O)C=2N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1OP(O)(O)=O WTIFIAZWCCBCGE-UUOKFMHZSA-N 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 229940071676 hydroxypropylcellulose Drugs 0.000 description 1
- 230000003116 impacting effect Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 235000010187 litholrubine BK Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- WNWZKKBGFYKSGA-UHFFFAOYSA-N n-(4-chloro-2,5-dimethoxyphenyl)-2-[[2,5-dimethoxy-4-(phenylsulfamoyl)phenyl]diazenyl]-3-oxobutanamide Chemical compound C1=C(Cl)C(OC)=CC(NC(=O)C(N=NC=2C(=CC(=C(OC)C=2)S(=O)(=O)NC=2C=CC=CC=2)OC)C(C)=O)=C1OC WNWZKKBGFYKSGA-UHFFFAOYSA-N 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- MTZWHHIREPJPTG-UHFFFAOYSA-N phorone Chemical compound CC(C)=CC(=O)C=C(C)C MTZWHHIREPJPTG-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000193 polymethacrylate Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- XWZDJOJCYUSIEY-YOYNBWDYSA-L procion red MX-5B Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=CC(NC=3N=C(Cl)N=C(Cl)N=3)=C2C(O)=C1\N=N\C1=CC=CC=C1 XWZDJOJCYUSIEY-YOYNBWDYSA-L 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
- FZUOVNMHEAPVBW-UHFFFAOYSA-L quinoline yellow ws Chemical compound [Na+].[Na+].O=C1C2=CC=CC=C2C(=O)C1C1=NC2=C(S([O-])(=O)=O)C=C(S(=O)(=O)[O-])C=C2C=C1 FZUOVNMHEAPVBW-UHFFFAOYSA-L 0.000 description 1
- WXQMFIJLJLLQIS-UHFFFAOYSA-N reactive blue 21 Chemical compound [Cu+2].C1=CC(S(=O)(=O)CCO)=CC=C1NS(=O)(=O)C1=CC=C2C([N-]3)=NC(C=4C5=CC=C(C=4)S(O)(=O)=O)=NC5=NC(C=4C5=CC=C(C=4)S(O)(=O)=O)=NC5=NC([N-]4)=C(C=C(C=C5)S(O)(=O)=O)C5=C4N=C3C2=C1 WXQMFIJLJLLQIS-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 229940099373 sudan iii Drugs 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229960000943 tartrazine Drugs 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- ZZHYREJHWJCRBB-UHFFFAOYSA-K trisodium 5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-[(1-sulfonatonaphthalen-2-yl)diazenyl]naphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[Na+].Oc1c(N=Nc2ccc3ccccc3c2S([O-])(=O)=O)c(cc2cc(cc(Nc3nc(Cl)nc(Cl)n3)c12)S([O-])(=O)=O)S([O-])(=O)=O ZZHYREJHWJCRBB-UHFFFAOYSA-K 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical class [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
Definitions
- the present invention is directed to ink compositions. More specifically, the present invention is directed to aqueous based ink compositions suitable for use in ink jet printing systems.
- Ink jet printing systems generally are of two types: continuous stream and drop-on-demand.
- continuous stream ink jet systems ink is emitted in a continuous stream under pressure through at least one orifice or nozzle. The stream is perturbed, causing it to break up into droplets at a fixed distance from the orifice. At the break-up point, the droplets are charged in accordance with digital data signals and passed through an electrostatic field which adjusts the trajectory of each droplet in order to direct it to a gutter for recirculation or a specific location on a recording medium.
- drop-on-demand systems a droplet is expelled from an orifice directly to a position on a recording medium in accordance with digital data signals. A droplet is not formed or expelled unless it is to be placed on the recording medium.
- drop-on-demand systems require no ink recovery, charging, or deflection, the system is much simpler than the continuous stream type.
- drop-on-demand ink jet systems There are two types of drop-on-demand ink jet systems.
- One type of drop-on-demand system has as its major components an ink filled channel or passageway having a nozzle on one end and a piezoelectric transducer near the other end to produce pressure pulses.
- the relatively large size of the transducer prevents close spacing of the nozzles, and physical limitations of the transducer result in low ink drop velocity. Low drop velocity seriously diminishes tolerances for drop velocity variation and directionality, thus impacting the system's ability to produce high quality copies.
- Drop-on-demand systems which use piezoelectric devices to expel the droplets also suffer the disadvantage of a slow printing speed.
- the other type of drop-on-demand system is known as thermal ink jet, or bubble jet, and produces high velocity droplets and allows very close spacing of nozzles.
- the major components of this type of drop-on-demand system are an ink filled channel having a nozzle on one end and a heat generating resistor near the nozzle.
- Printing signals representing digital information originate an electric current pulse in a resistive layer within each ink passageway near the orifice or nozzle, causing the ink in the immediate vicinity to evaporate almost instantaneously and create a bubble.
- the ink at the orifice is forced out as a propelled droplet as the bubble expands.
- the drop-on-demand ink jet printers provide simpler, lower cost devices than their continuous stream counterparts, and yet have substantially the same high speed printing capability.
- the operating sequence of the bubble jet system begins with a current pulse through the resistive layer in the ink filled channel, the resistive layer being in close proximity to the orifice or nozzle for that channel. Heat is transferred from the resistor to the ink. The ink becomes superheated far above its normal boiling point, and for water based ink, finally reaches the critical temperature for bubble formation or nucleation of around 280°C. Once nucleated, the bubble or water vapor thermally isolates the ink from the heater and no further heat can be applied to the ink. This bubble expands until all the heat stored in the ink in excess of the normal boiling point diffuses away or is used to convert liquid to vapor, which removes heat due to heat of vaporization.
- the expansion of the bubble forces a droplet of ink out of the nozzle, and once the excess heat is removed, the bubble collapses on the resistor. At this point, the resistor is no longer being heated because the current pulse has passed and, concurrently with the bubble collapse, the droplet is propelled at a high rate of speed in a direction towards a recording medium.
- the resistive layer encounters a severe cavitational force by the collapse of the bubble, which tends to erode it.
- the ink channel refills by capillary action. This entire bubble formation and collapse sequence occurs in about 10 microseconds.
- the channel can be refired after 100 to 500 microseconds minimum dwell time to enable the channel to be refilled and to enable the dynamic refilling factors to become somewhat dampened.
- Thermal ink jet processes are well known and are described in, for example, U.S. Patent 4,601,777, U.S. Patent 4,251,824, U.S. Patent 4,410,899, U.S. Patent 4,412,224, and U.S. Patent 4,532,530, the disclosures of each of which are totally incorporated herein by reference.
- Known ink jet inks generally comprise a water soluble dye which is soluble in an ink vehicle such as water or a mixture comprising water and a water soluble or water miscible organic solvent.
- an ink vehicle such as water or a mixture comprising water and a water soluble or water miscible organic solvent.
- U.S. Patent 4,184,881 (Bradley) discloses an ink composition for use in ink jet printing comprising an aqueous solution of a water soluble dye and a humectant consisting of ethylene oxide adducts of at least one acetylenic diol in the absence of any glycol or glycol ether.
- Patent 4,337,183 discloses an aqueous printing ink composition which comprises a physical mixture of polyurethane resin, polyethylene resin, and water as the vehicle.
- the invention provides a family of water based inks with enhanced physical and mechanical properties, superior abrasion resistance, and good adhesion to various substrates.
- U.S. Patent 3,477,862 discloses an ink comprising a dyestuff, a solution of high molecular weight polyethylene oxide and glycerin for employment in a pen, nozzle or other ink applying means to ensure the inscription of a clear continuous solid line on a chart on which the ink applying means is associated as the ink applying means traverses the chart.
- Heterophase ink jet inks are also known.
- U.S. Patent 4,014,833 discloses a composition and method for improving the ink transfer properties of aqueous printing inks.
- the composition is an aqueous ink containing from 0.1 to 1.5 percent by weight of a polyethylene oxide resin having a molecular weight in the range of from 100,000 to 350,000.
- U.S. Patent 4,680,332 discloses a heterophase ink composition which comprises a water insoluble polymer dispersed in a liquid medium, the polymer containing therein an oil soluble dye, and a nonionic stabilizer permanently attached thereto.
- the polymer may include styrene, parachlorostyrene, vinyl naphthalene, and acrylates wherein the carbon chain length is from about 1 to about 18 carbon atoms.
- the stabilizers may include ethylene oxide and propylene oxide block copolymers.
- U.S. Patent 4,705,567 discloses a heterophase ink jet ink composition which comprises water and a dye covalently attached to a component selected from the group consisting of poly(ethylene glycols) and poly(ethylene imines), which component is complexed with a heteropolyanion.
- U.S. Patent 4,705,567 discloses a heterophase ink jet ink composition which comprises water and a dye covalently attached to a component selected from the group consisting of poly(ethylene glycols) and poly(ethylene imines), which component is complexed with a heteropolyanion.
- Patent 4,597,794 discloses an ink jet recording process which comprises forming droplets of an ink and recording on an image receiving material by using the droplets, wherein the ink is prepared by dispersing fine particles of a pigment into an aqueous dispersion medium containing a polymer having both a hydrophilic and a hydrophobic construction portion.
- the hydrophilic portion constitutes a polymer of monomers having mainly polymerizable vinyl groups into which hydrophilic portions such as carboxylic acid groups, sulfonic acid groups, sulfate groups, and the like are introduced.
- Pigment particle size may be from several microns to several hundred microns.
- the ink compositions disclosed may also include additives such as surfactants, salts, resins, and dyes.
- ink compositions that when used in ink jet printing processes result in few or no detectable missing drops. Further, a need remains for ink compositions that when used in ink jet printing processes result in reduced drop satellites; drop satellites are secondary drops that issue from the nozzle or channel after the primary drop has been ejected, resulting in undesired spots on the receiver sheet. Additionally, there is a need for ink compositions having the above advantages accompanied by acceptable latency, surface tension, and viscosity values. There is also a need for ink jet printing processes with inks exhibiting the above noted advantages. A need also exists for thermal ink jet printing processes using inks exhibiting the above noted advantages.
- ink compositions that exhibit short drop transit times and enable good drop directionality when used in thermal ink jet printing processes. Additionally, there is a need for ink compositions that result in reduced or eliminated jitter when used in thermal ink jet printing processes; jitter refers to the degree of variation in drop speed, and reduced jitter entails more uniform drop speeds during the printing process.
- the present invention provides an ink composition which comprises an aqueous liquid vehicle, a colorant, and a polymeric additive of the formula wherein R1 and R2 are independently selected from the group consisting of hydrogen, alkyl groups with from 1 to 8 carbon atoms, and alkoxy groups with from 1 to 8 carbon atoms, R3 and R4 are independently selected from the group consisting of alkyl groups with from 1 to 4 carbon atoms, and x and y are each independently a number of from 100 to 400, present in an amount of at least 1 part per million.
- Another embodiment of the present invention is directed to a process which comprises incorporating into an ink jet printing apparatus an ink which comprises an aqueous liquid vehicle, a colorant, and a polymeric additive of the formula wherein R1 and R2 are independently selected from the group consisting of hydrogen, alkyl groups with from 1 to 8 carbon atoms, and alkoxy groups with from 1 to 8 carbon atoms, R3 and R4 are independently selected from the group consisting of alkyl groups with from 1 to 4 carbon atoms, and x and y are each independently a number of from 100 to 400, present in an amount of at least 1 part per million, and causing droplets of the ink composition to be ejected in an imagewise pattern onto a substrate.
- the printing apparatus employs a thermal ink jet process, wherein the droplets of ink are caused to be ejected by heating the ink and causing bubbles to form therein.
- the liquid vehicle of the inks may consist of water, or it may comprise a mixture of water and a miscible organic component, such as ethylene glycol, propylene glycol, diethylene glycols, glycerine, dipropylene glycols, polyethylene glycols, polypropylene glycols, amides, ethers, carboxylic acids, esters, alcohols, organosulfides, organosulfoxides, sulfones, alcohol derivatives, carbitol, butyl carbitol, cellusolve, ether derivatives, amino alcohols, ketones, N-methylpyrrolidinone cyclohexylpyrrolidone, hydroxyethers, amides, sulfoxides, lactones, and other water miscible materials, as well as mixtures thereof.
- a miscible organic component such as ethylene glycol, propylene glycol, diethylene glycols, glycerine, dipropylene glycols, polyethylene glycols
- the water to organic ratio may be in any effective range, and typically is from 100:0 to 30:70, preferably from 97:3 to 50:50, although the ratio can be outside this range.
- the non-water component of the liquid vehicle generally serves as a humectant which has a boiling point higher than that of water (100°C).
- the liquid vehicle (comprising water plus humectant) is generally present in an amount of from 60 to 99.5 percent by weight, and preferably from 75 to 99 percent by weight, although the amount can be outside of this range.
- Inks in embodiments of the present invention contain a colorant.
- any effective dye such as one of the direct dyes or the acid dyes, can be selected as the colorant, provided that it is compatible with the other ink components and is soluble in the liquid vehicle.
- suitable dyes include Bernacid Red 2BMN, Pontamine Brilliant Bond Blue A, BASF X34, Pontamine, Food Black 2, Carodirect Turquoise FBL Supra Conc.
- Dyes that are invisible to the naked eye but detectable when exposed to radiation outside the visible wavelength range such as ultraviolet or infrared radiation
- dansyl-lysine N-(2-aminoethyl)-4-amino-3,6-disulfo-1,8-dinaphthalimide dipotassium salt, N-(2-aminopentyl)-4-amino-3,6-disulfo-1,8-dinaphthalimide dipotassium salt
- Cascade Blue ethylenediamine trisodium salt available from Molecular Proes, Inc.
- Cascade Blue cadaverine trisodium salt available from Molecular Proes, Inc.
- bisdiazinyl derivatives of 4,4'-diaminostilbene-2,2'-disulfonic acid amide derivatives of 4,4'-diaminostilbene-2,2'-disulfonic acid
- the dye is present in the ink composition in any effective amount, generally from 1 to 15 percent by weight, and preferably from 2 to 7 percent by weight (wherein the amount refers to the amount of dye molecules present in the ink), although the amount can be outside of this range.
- the colorant for the ink compositions in embodiments of the present invention can be a pigment, or a mixture of one or more dyes and/or one or more pigments.
- the pigment can be black, cyan, magenta, yellow, red, blue, green, brown, mixtures thereof, and the like.
- suitable black pigments include various carbon blacks such as channel black, furnace black, lamp black, and the like.
- Colored pigments include red, green, blue, brown, magenta, cyan, and yellow particles, as well as mixtures thereof.
- magenta pigments include 2,9-dimethyl-substituted quinacridone and anthraquinone dye, identified in the Color Index as CI 60710, CI Dispersed Red 15, a diazo dye identified in the Color Index as CI 26050, CI Solvent Red 19, and the like.
- suitable cyan pigments include copper tetra-4-(octadecyl sulfonamido) phthalocyanine, X-copper phthalocyanine pigment, listed in the Color Index as CI 74160, CI Pigment Blue, and Anthradanthrene Blue, identified in the Color Index as CI 69810, Special Blue X-2137, and the like.
- yellow pigments that can be selected include diarylide yellow 3,3-dichlorobenzidene acetoacetanilides, a monoazo pigment identified in the Color Index as CI 12700, CI Solvent Yellow 16, a nitrophenyl amine sulfonamide identified in the Color Index as Foron Yellow SE/GLN, CI Dispersed Yellow 33, 2,5-dimethoxy-4-sulfonanilide phenylazo-4'-chloro-2,5-dimethoxy acetoacetanilide, Permanent Yellow FGL, and the like.
- diarylide yellow 3,3-dichlorobenzidene acetoacetanilides a monoazo pigment identified in the Color Index as CI 12700
- CI Solvent Yellow 16 a nitrophenyl amine sulfonamide identified in the Color Index as Foron Yellow SE/GLN
- CI Dispersed Yellow 33 2,5-dimethoxy-4-sulfonanilide phenylazo-4'-ch
- pigments include Normandy Magenta RD-2400 (Paul Uhlich), Paliogen Violet 5100 (BASF), Paliogen Violet 5890 (BASF), Permanent Violet VT2645 (Paul Uhlich), Heliogen Green L8730 (BASF), Argyle Green XP-111-S (Paul Uhlich), Brilliant Green Toner GR 0991 (Paul Uhlich), Heliogen Blue L6900, L7020 (BASF), Heliogen Blue D6840, D7080 (BASF), Sudan Blue OS (BASF), PV Fast Blue B2G01 (American Hoechst), Irgalite Blue BCA (Ciba-Geigy), Paliogen Blue 6470 (BASF), Sudan III (Matheson, Coleman, Bell), Sudan II (Matheson, Coleman, Bell), Sudan IV (Matheson, Coleman, Bell), Sudan Orange G (Aldrich), Sudan Orange 220 (BASF), Paliogen Orange 3040 (BASF), Ortho Orange OR 2673 (Paul Uhlich), Paliogen Yellow
- pigments can also be selected.
- the pigment particle size is as small as possible to enable a stable colloidal suspension of the particles in the liquid vehicle and to prevent clogging of the ink channels when the ink is used in a thermal ink jet printer.
- Preferred particle average diameters are generally from 0.001 to 0.1 micrometer (micron).
- the pigment is present in the ink composition in any effective amount, generally from 1 to 7 percent by weight and preferably from 2 to 5 percent by weight, although the amount can be outside of this range.
- the ink compositions in embodiments of the present invention also contain a polymeric additive consisting of two polyalkylene oxide chains bound to a central bisphenol-A moiety.
- This additive is of the formula wherein R1 and R2 are independently selected from the group consisting of hydrogen, alkyl groups with from 1 to 8 carbon atoms, such as methyl, ethyl, propyl, and the like, and alkoxy groups with from 1 to 8 carbon atoms, such as methoxy, ethoxy, butoxy, and the like, R3 and R4 are independently selected from the group consisting of alkyl groups with from 1 to 4 carbon atoms, and x and y are each independently a number of from 100 to 400, and preferably from 100 to 200.
- the molecular weight of the polyalkylene oxide/bisphenol-A polymer is from 14,000 to 22,000, and preferably from about 15,000 to 20,000, although the molecular weight can be outside this range.
- Materials of this formula are commercially available; for example, Carbowax M20, a polyethylene oxide/bisphenol-A polymer of the above formula with a molecular weight of about 18,000, available from Union Carbide Corporation, Danbury, CT, is a suitable polymeric additive for the inks of the present invention.
- compounds of the above formula can be prepared by the methods disclosed in Polyethers , N. G. Gaylord, John Wiley & Sons, New York (1963) and "Laboratory Synthesis of Polyethylene Glycol Derivatives," J.
- the polyalkylene oxide/bisphenol-A additive is generally present in the ink in an amount of at least 1 part per million. Typically, the polyalkylene oxide/bisphenol-A additive is present in amounts of up to 1 percent by weight of the ink, and preferably in amounts of up to 0.5 percent by weight of the ink; larger amounts of the additive may increase the viscosity of the ink beyond the desired level, but larger amounts can be used in applications wherein increased ink viscosity is not a problem.
- additives can also be present in the inks of embodiments of the present invention.
- one or more surfactants or wetting agents can be added to the ink.
- These additives may be of the cationic, anionic, or nonionic types.
- Suitable surfactants and wetting agents include sodium lauryl sulfate, Tamol® SN, Tamol® LG, those of the Triton® series available from Rohm and Haas Company, those of the Marasperse® series, those of the Igepal® series available from GAF Company, those of the Tergitol® series, and other commercially available surfactants.
- These surfactants and wetting agents are present in effective amounts, generally from 0 to about 15 percent by weight, and preferably from about 0.01 to about 8 percent by weight, although the amount can be outside of this range.
- Polymeric additives can also be added to the inks of the present invention to enhance the viscosity of the ink and the stability of the pigment particles and to reduce the rate of agglomeration and precipitation of the particles.
- Water soluble polymers such as Gum Arabic, polyacrylate salts, polymethacrylate salts, polyvinyl alcohols, hydroxy propylcellulose hydroxyethylcellulose, polyvinylpyrrolidinone polyvinylether, starch, polysaccharides, and the like are particularly useful for stabilizing pigment particles in a water based liquid vehicle such as water or a mixture of water and a water miscible organic liquid.
- Polymeric stabilizers may be present in the ink of the present invention in amounts of from 0 to 10 percent by weight, and preferably from 0.01 to 5 percent by weight, although the amount can be outside of this range.
- biocides such as Dowicil 150, 200, and 75, benzoate salts, sorbate salts, and the like, present in an amount of from 0.0001 to 4 percent by weight, and preferably from 0.01 to 2.0 percent by weight, pH controlling agents such as acids or, bases, phosphate salts, carboxylates salts, sulfite salts, amine salts, and the like, present in an amount of from 0 to 1 percent by weight and preferably from 0.01 to 1 percent by weight, or the like.
- biocides such as Dowicil 150, 200, and 75, benzoate salts, sorbate salts, and the like, present in an amount of from 0.0001 to 4 percent by weight, and preferably from 0.01 to 2.0 percent by weight
- pH controlling agents such as acids or, bases, phosphate salts, carboxylates salts, sulfite salts, amine salts, and the like, present in an amount of from 0 to 1 percent by weight and preferably from 0.01 to 1 percent by weight, or
- the ink compositions of the present invention are generally of a viscosity suitable for use in thermal ink jet printing processes.
- the ink viscosity is no more than about 5 centipoise, and preferably is from 1 to 2.5 m Pas (centipoise).
- Ink compositions in embodiments of the present invention can be prepared by any suitable process.
- the inks are prepared by simple mixing of the ingredients.
- One process entails mixing all of the ink ingredients together and filtering the mixture to obtain an ink.
- Inks of the present invention can be prepared by preparing a conventional ink composition according to any desired process, such as by mixing the ingredients, heating if desired, and filtering, followed by adding the ink additive of the present invention to the mixture and mixing at room temperature with moderate shaking until a homogeneous mixture is obtained, typically from about 5 to about 10 minutes.
- the ink additive of the present invention can be mixed with the other ink ingredients during the ink preparation process, which takes place according to any desired procedure, such as by mixing all the ingredients, heating if desired, and filtering.
- the present invention is also directed to a process which entails incorporating an ink composition of the present invention into an ink jet printing apparatus and causing droplets of the ink composition to be ejected in an imagewise pattern onto a substrate.
- the printing apparatus employs a thermal ink jet process wherein the ink in the nozzles is selectively heated in an imagewise pattern, thereby causing droplets of the ink to be ejected in imagewise pattern.
- any suitable substrate can be employed, including plain papers such as Xerox® 4024 papers, ruled notebook paper, bond paper, silica coated papers such as Sharp Company silica coated paper, JuJo paper, and the like, transparency materials, fabrics, textile products, plastics, polymeric films, inorganic substrates such as metals and wood, and the like.
- the process entails printing onto a porous or ink absorbent substrate, such as plain paper.
- An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, NY, 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, NJ), 1 percent by weight of sodium lauryl sulfate (obtained from Fisher Scientific, Fair Lawn, NJ), and 81.5 percent by weight of deionized water was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering.
- Tartrazine FD&C Yellow #5 a yellow dye obtained from Buffalo Color, West Patterson, NY
- 15 percent by weight of cyclohexyl pyrrolidone obtained from GAF Corporation, Wayne, NJ
- 1 percent by weight of sodium lauryl sulfate obtained from Fisher Scientific, Fair Lawn, NJ
- 81.5 percent by weight of deionized water was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering.
- Two additional inks were also prepared, said inks being of the same composition as the first except that one contained 0.1 percent by weight of Carbowax M20 (a polyethylene oxide/bisphenol-A polymer of the formula with a molecular weight of 18,000, obtained from Union Carbide Corporation, Danbury, CT) and the other contained 0.3 percent by weight of Carbowax M20.
- Carbowax M20 was added to the ink at room temperature and the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution.
- An ink composition containing 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, NY, 15 percent by weight of ethylene glycol, 0.3 percent by weight of Carbowax M20, and 82.2 percent by weight of water was prepared by mixing together the ingredients at room temperature, stirring for about 10 minutes to obtain a homogeneous solution, and filtering.
- the ink thus prepared was incorporated into a jetting test fixture having 300 spots per inch with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Drop Speed (Transit Time - microseconds) 70 55 170 55 400 60 800 57 1700 59 2400 59 3200 64 4000 69 5000 69 5500 68 5800 72 6000 74 6200 75 6300 75 Frequency (Hertz) Drop Volume (picoliters) 1000 118 2000 116 3500 121 6000 128 8000 125 8500 110 9000 96 As the data indicate, the frequency response in terms of both drop volume and drop speed was nearly flat up to a frequency of about 5000, which is generally regarded as the maximum usable frequency. In addition, the drop volume was measured up to about 130 picoliters, which was almost twice that observed for an ink of similar composition but
- An ink composition containing 6 percent by weight of Special Black 7984 (Food Black #2), a black dye obtained from Mobay Chemical Company, 15 percent by weight of cyclohexyl pyrrolidone, obtained from GAF Corporation, Wayne, NJ, 1 percent by weight of sodium lauryl sulfate (obtained from Fisher Scientific, Fair Lawn, NJ), and 78 percent by weight of water was prepared by mixing together the ingredients at room temperature, stirring for about 10 minutes to obtain a homogeneous solution, and filtering.
- Another ink of the same composition except that it contained 0.1 percent by weight of Carbowax M20 was prepared by adding the appropriate amount of Carbowax M20 to an aliquot of the first ink.
- An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, NY, 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, NJ), and 82.5 percent by weight of deionized water was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering.
- An additional ink was also prepared, said ink being of the same composition as the first except that it contained 0.3 percent by weight of Carbowax M20.
- the Carbowax M20 was added to the ink at room temperature and the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution.
- the inks thus prepared were incorporated into a jetting test fixture having 300 spots per 25,40 mm (inch) with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Drop Speed (Transit Time - microseconds) Drop Speed Standard Deviation 70 60.48 0.93 140 60.64 1.17 350 62.24 1.85 700 69.08 4.62 1400 68.43 2.17 2100 73.17 5.34 2800 75.11 5.95 3500 77.32 5.64 4200 80.06 6.09 4900 77.39 6.74 5180 76.85 6.84 5460 76.66 8.23 5740 69.24 5.80 6020 66.44 4.11 6300 68.67 6.54 6440 66.16 5.92 6580 67.20 6.66 6720 64.84 6.90 6860 61.79 3.65 7000
- Another ink of the same composition except that it contained 0.1 percent by weight of Carbowax M20 was prepared by adding the appropriate amount of Carbowax M20 to an aliquot of the first ink.
- the ink thus prepared was incorporated into a jetting test fixture having 300 spots per inch with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Frequency (Hertz) Drop Speed (Transit Time - microseconds) Drop Speed Standard Deviation 70 89.93 4.79 140 94.31 7.53 350 111.63 7.13 700 119.50 6.71 1400 130.65 7.93 2100 139.32 9.39 2800 144.07 10.83 3500 163.89 20.67 4200 181.03 12.06 4900 141.69 52.03 5180 94.16 67.65 5460 43.33 57.79 5740 23.54 37.09 6020 17.77 23.44 6300 14.66 14.26 6440 17.77 13.47 6580 15.15 12.47 6720 19.62 13.95 6860 22.24 15.79 7000 22.04 15.
- the ink thus prepared was incorporated into a jetting test fixture having 300 spots per inch with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Drop Speed (Transit Time - microseconds) Drop Speed Standard Deviation 70 75.09 3.31 140 76.50 4.57 350 87.80 7.25 700 94.57 8.34 1400 105.08 7.82 2100 111.84 9.05 2800 114.50 8.06 3500 119.72 8.71 4200 130.30 9.77 4900 132.50 10.26 5180 129.21 10.30 5460 122.24 9.62 5740 119.89 8.79 6020 115.32 7.77 6300 110.80 6.52 6440 109.14 6.88 6580 106.30 6.83 6720 104.78 5.29 6860 103.53 5.65 7000 101.25 5.44 As the
- An ink composition comprising 5 percent by weight of Special Black 7984 (Food Black #2), a black dye obtained from Mobay Chemical Company, 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, NJ), 0.5 percent by weight of sodium lauryl sulfate (obtained from Fisher Scientific, Fair Lawn, NJ), 79.48 percent by weight of deionized water, and 0.02 percent by weight of polyethyene oxide of the formula HO(CH2CH2O) n H wherein n is about 2272, with a molecular weight of about 100,000 (obtained from Union Carbide Corporation, Danbury, CT) was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering.
- Special Black 7984 Food Black #2
- a black dye obtained from Mobay Chemical Company
- cyclohexyl pyrrolidone obtained from GAF Corporation, Wayne, NJ
- sodium lauryl sulfate obtained
- the ink thus prepared was incorporated into a jetting test fixture having 300 spots per inch with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Drop Speed (Transit Time - microseconds) Drop Speed Standard Deviation 70 72.66 2.03 140 74.15 2.92 350 80.05 4.69 700 91.07 5.82 1400 108.57 7.71 2100 113.34 6.90 2800 115.86 7.64 3500 102.55 7.22 4200 95.77 11.67 4900 98.44 8.75 5180 97.56 9.72 5460 96.66 10.34 5740 98.10 10.00 6020 94.31 11.67 6300 92.35 11.52 6440 90.93 10.22 6580 89.52 12.97 6720 90.06 13.08 6860 86.31 16.51 7000 77.34 25.11 As the
- An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, NY, 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, NJ), 1 percent by weight of sodium lauryl sulfate (obtained from Fisher Scientific, Fair Lawn, NJ), 81.2 percent by weight of deionized water, and 0.3 percent by weight of methylated polyethylene glycol of the formula CH3O(CH2CH2O) n H wherein n is about 112, with a molecular weight of 5000 (obtained from Union Carbide Corporation, Danbury, CT) was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering.
- the ink thus prepared was incorporated into a jetting test fixture having 300 spots per inch with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Drop Speed (Transit Time - microseconds) Drop Speed Standard Deviation 70 85.38 4.76 140 90.46 6.72 350 110.22 9.43 700 114.11 7.79 1400 126.44 10.25 2100 136.43 11.08 2800 145.78 13.77 3500 146.98 11.89 4200 162.58 13.24 4900 157.14 15.47 5180 151.27 9.25 5460 137.47 24.34 5740 97.45 56.86 6020 86.14 54.49 6300 78.28 51.94 6440 25.34 42.15 6580 63.77 46.98 6720 26.99 39.49 6860 29.06 35.84 7000 15.43 16.
- An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, NY, 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, NJ), 1 percent by weight of sodium lauryl sulfate (obtained from Fisher Scientific, Fair Lawn, NJ), 81.2 percent by weight of deionized water, and 0.3 percent by weight of polyethylene oxide of the formula HO(CH2CH2O) n H wherein n is about 14, with a molecular weight of 600 (obtained from Union Carbide Corporation, Danbury, CT) was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering.
- the ink thus prepared was incorporated into a jetting test fixture having 300 spots per inch with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Drop Speed (Transit Time - microseconds) Drop Speed Standard Deviation 70 78.72 4.54 140 84.82 6.36 350 96.97 7.96 700 105.43 7.55 1400 118.02 8.11 2100 127.71 10.63 2800 136.52 11.05 3500 127.96 10.07 4200 125.60 15.75 4900 123.62 12.85 5180 123.57 13.26 5460 115.55 13.31 5740 117.35 12.61 6020 112.33 12.07 6300 109.15 10.85 6440 104.63 15.19 6580 103.65 9.54 6720 96.87 16.40 6860 86.57 29.08 7000 69.
- An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, NY, 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, NJ), 1 percent by weight of sodium lauryl sulfate (obtained from Fisher Scientific, Fair Lawn, NJ), 81.48 percent by weight of deionized water, and 0.02 percent by weight of polyethylene oxide of the formula HO(CH2CH2O) n H wherein n is about 2272, with a molecular weight of 100,000 (obtained from Union Carbide Corporation, Danbury, CT) was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering.
- the ink thus prepared was incorporated into a jetting test fixture having 300 spots per inch with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Drop Speed (Transit Time - microseconds) Drop Speed Standard Deviation 70 84.90 2.91 140 88.29 4.28 350 98.24 9.02 700 110.74 8.38 1400 117.73 8.23 2100 130.01 9.25 2800 138.17 12.75 3500 146.19 15.40 4200 156.23 16.24 4900 134.08 12.19 5180 134.58 11.99 5460 137.30 10.58 5740 123.01 27.28 6020 73.77 55.24 6300 39.33 48.53 6440 32.24 41.50 6580 30.46 41.16 6720 30.08 35.83 6860 16.12 19.77 7000 12.51 11.42
- An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, NY, 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, NJ), 1 percent by weight of sodium lauryl sulfate (obtained from Fisher Scientific, Fair Lawn, NJ), 81.4 percent by weight of deionized water, and 0.1 percent by weight of polyethylene oxide of the formula HO(CH2CH2O) n H wherein n is about 2272, with a molecular weight of 100,000 (obtained from Union Carbide Corporation, Danbury, CT) was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering.
- the ink thus prepared was incorporated into a jetting test fixture having 300 spots per inch with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Drop Speed (Transit Time - microseconds) Drop Speed Standard Deviation 70 81.92 4.96 140 87.64 5.97 350 93.65 6.96 700 107.63 6.68 1400 116.95 8.18 2100 124.50 99.81 2800 130.03 10.79 3500 136.76 10.20 4200 143.96 11.02 4900 148.08 11.80 5180 144.48 9.67 5460 137.51 7.97 5740 131.48 7.37 6020 124.43 20.03 6300 113.30 28.09 6440 108.05 26.52 6580 107.08 25.80 6720 111.04 6.21 6860 99.23 29.77
- An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, NY, 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, NJ), 1 percent by weight of sodium lauryl sulfate (obtained from Fisher Scientific, Fair Lawn, NJ), 81 percent by weight of deionized water, and 0.5 percent by weight of polyethylene oxide of the formula HO(CH2CH2O) n H wherein n is about 2272, with a molecular weight of 100,000 (obtained from Union Carbide Corporation, Danbury, CT) was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering.
- the ink thus prepared was incorporated into a jetting test fixture having 300 spots per inch with a heater voltage applied at about 38 volts (about 10 percent above the minimum voltage required to fire drops of the ink).
- the drop speed to travel 0.5 millimeter was then measured as a function of frequency with the following results: Frequency (Hertz) Drop Speed (Transit Time - microseconds) Drop Speed Standard Deviation 70 78.60 3.08 140 79.64 4.12 350 95.58 7.98 700 107.38 7.51 1400 115.97 8.50 2100 118.69 10.34 2800 119.55 10.18 3500 112.81 10.39 4200 103.96 10.58 4900 95.75 9.41 5180 95.38 9.96 5460 92.45 10.99 5740 89.28 10.97 6020 88.23 11.52 6300 84.94 10.59 6440 83.12 11.77 6580 79.98 13.47 6720 76.98 12.02 6860 72.99 13.99 7000 71.07 14.12 As the data
Claims (11)
- Tintenzusammensetzung, welche eine wäßrige Trägerflüssigkeit und ein Färbemittel umfaßt, gekennzeichnet durch einen polymeren Zusatz der Formel
- Tintenzusammensetzung gemäß Anspruch 1, dadurch gekennzeichnet, daß x und y unabhängig voneinander eine Zahl von 100 bis 200 ist.
- Tintenzusammensetzung gemäß den Ansprüchen 1 oder 2, dadurch gekennzeichnet, daß der polymere Zusatz in einer Menge von 0,0001 Gewichts-% bis 1 Gewichts-% enthalten ist.
- Tintenzusammensetzung gemäß den Ansprüchen 1 oder 2, dadurch gekennzeichnet, daß der polymere Zusatz in einer Menge von 0,0001 Gewichts-% bis 0,5 Gewichts-% enthalten ist.
- Tintenzusammensetzung gemäß einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, daß die wäßrige Trägerflüssigkeit Wasser und ein Feuchthaltemitte enthält.
- Tintenzusammensetzung gemäß einem der Ansprüche 1 bis 6, dadurch gekennzeichnet, daß die Trägerflüssigkeit in einer Menge von 75 bis 99 Gewichts-% und der Farbstoff in einer Menge von 1 bis 15 Gewichts-% enthalten ist.
- Tintenzusammensetzung gemäß einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, daß der polymere Zusatz ein Molekulargewicht von etwa 14000 bis etwa 22000 aufweist.
- Tintenzusammensetzung gemäß einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, daß die Viskosität der Tinte 1 bis 5 mPas beträgt.
- Tintenzusammensetzung gemäß Anspruch 6, in der das Feuchthaltemittel Cyclohexylpyrrolidon ist.
- Ein Verfahren welches das Einbringen einer Tintenzusammensetzung in einen Tintenstrahldrucker, dadurch gekennzeichnet, daß die Tinte wie in einem der Ansprüche 1 bis 10 beansprucht ist, und das Spritzen von Tröpfchen der Tintenzusammensetzung in bildmäßiger Verteilung auf ein Substrat umfaßt.
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Application Number | Priority Date | Filing Date | Title |
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US738021 | 1991-07-30 | ||
US07/738,021 US5207825A (en) | 1991-07-30 | 1991-07-30 | Ink compositions for ink jet printing |
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EP0525994A1 EP0525994A1 (de) | 1993-02-03 |
EP0525994B1 true EP0525994B1 (de) | 1995-04-12 |
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EP92306061A Expired - Lifetime EP0525994B1 (de) | 1991-07-30 | 1992-07-01 | Tintenzusammensetzungen für das Ink-Jet-Schreibverfahren |
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US (1) | US5207825A (de) |
EP (1) | EP0525994B1 (de) |
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DE (1) | DE69202021T2 (de) |
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Publication number | Priority date | Publication date | Assignee | Title |
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DE69427068T2 (de) * | 1993-11-30 | 2001-10-25 | Seiren Co Ltd | Tinte für Tintenstrahlfärbung und Verfahren zur Herstellung von Mischfarben |
US5627578A (en) * | 1995-02-02 | 1997-05-06 | Thermotek, Inc. | Desk top printing of raised text, graphics, and braille |
CA2211113A1 (en) * | 1995-02-03 | 1996-08-08 | Videojet Systems International, Inc. | An ink composition |
US5594044A (en) * | 1995-03-03 | 1997-01-14 | Videojet Systems International, Inc. | Ink jet ink which is rub resistant to alcohol |
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-
1991
- 1991-07-30 US US07/738,021 patent/US5207825A/en not_active Expired - Lifetime
-
1992
- 1992-07-01 DE DE69202021T patent/DE69202021T2/de not_active Expired - Lifetime
- 1992-07-01 EP EP92306061A patent/EP0525994B1/de not_active Expired - Lifetime
- 1992-07-23 JP JP4196688A patent/JPH0726050B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
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JPH0726050B2 (ja) | 1995-03-22 |
US5207825A (en) | 1993-05-04 |
JPH05194887A (ja) | 1993-08-03 |
DE69202021D1 (de) | 1995-05-18 |
EP0525994A1 (de) | 1993-02-03 |
DE69202021T2 (de) | 1995-12-21 |
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